Cantrell Syndrome—A Rare Complex Congenital Anomaly: A Case Report and Literature Review

Mesenchymal Wnt signaling promotes formation of sternum and thoracic body wall

(2015) John Snowball et al.   DEVELOPMENTAL BIOLOGY

A rare case of cardiac anomaly: prenatally diagnosed ectopia cordis

(2015) Yalcin Celik et al.   TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS

Surgical treatment and outcomes of pentalogy of Cantrell in eight patients

(2014) Xueqin Zhang et al.   JOURNAL OF PEDIATRIC SURGERY

Co-occurrence of severe Goltz-Gorlin syndrome and pentalogy of Cantrell - Case report and review of the literature

(2011) Robert Smigiel et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Deletion of mouse Porcn blocks Wnt ligand secretion and reveals an ectodermal etiology of human focal dermal hypoplasia/Goltz syndrome

(2011) J. J. Barrott et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Phenotype and genotype in 17 patients with Goltz-Gorlin syndrome

(2009) S M Maas et al.   JOURNAL OF MEDICAL GENETICS

Embryology, sternal clefts, ectopia cordis, and Cantrell's pentalogy

(2008) Scott A. Engum   Seminars in Pediatric Surgery